Canonical Allele Identifier: CA1883176780
Gene: RXRA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408195C= , CM000671.2:g.134408195C= GRCh38
NC_000009.11:g.137300041C= , CM000671.1:g.137300041C= GRCh37
NC_000009.10:g.136439862C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.326C= MANE Select ENSP00000419692.1:p.Pro109=
ENST00000672570.1:c.245C= ENSP00000500402.1:p.Pro82=
ENST00000356384.4:n.736C=
ENST00000481739.1:c.326C= ENSP00000419692.1:p.Pro109=
NM_001291920.1:c.245C= NP_001278849.1:p.Pro82=
NM_001291921.1:c.35C= NP_001278850.1:p.Pro12=
NM_002957.5:c.326C= NP_002948.1:p.Pro109=
NM_002957.6:c.326C= MANE Select NP_002948.1:p.Pro109=
NM_001291921.2:c.35C= NP_001278850.1:p.Pro12=
NM_001291920.2:c.245C= NP_001278849.1:p.Pro82=